Cytochrome c synthesis inhibitors

ABSTRACT

The invention provides methods for identifying a compound that inhibits cytochrome c synthesis. This invention further provides a method for the high throughput screening of compounds that inhibit cytochrome c synthesis.

CROSS-REFERENCE TO RELATED APPLICATION

This application claims priority from Provisional Application Ser. No.60/821,053 filed on Aug. 1, 2006, which is hereby incorporated byreference in its entirety.

GOVERNMENTAL RIGHTS

This work was supported by the U.S. Department of Health and HumanServices/National Institutes of Health grant number 5R01 GM047909-11.The U.S. government has certain rights in this invention.

FIELD OF THE INVENTION

The present invention generally relates to screening methods for theidentification of compounds and compositions that inhibit cytochrome c.

BACKGROUND

The treatment of bacterial infections is a perpetual challenge in themedical community. Many powerful antibiotics exist that target differentaspects of bacterial physiology. Some classes of antibiotics are toxicto bacteria, while other classes of antibiotics arrest the propagationof the bacteria in the body, giving the immune system adequate time toeliminate the bacterial infection. Penicillins, bacitracin,cephalosporins, and vancomycin disrupt the process of cell walldevelopment in bacteria. Other antibiotics such as the aminoglycosides,chloramphenicol, erythromycin, clindamycin, tetracyclines, trimethoprim,and sulfanimides inhibit or disrupt some aspect of protein synthesis inthe targeted bacteria. Still other antibiotics such as quinolones andrifampin disrupt the process of DNA or RNA synthesis in bacteria.Although the antibiotics listed above represent a powerful arsenal oftreatments for bacterial infections, the increasingly widespread use ofthese antibiotics has resulted in the development of bacterial strainsthat are resistant to many of the currently available antibiotics.

Some treatment-resistant bacterial strains have plagued hospitals fordecades, such as Staphylococcus aureus (responsible for Staphinfections), Streptococcus pneumoniae (responsible for pneumonia andmeningitis), and Proteus vulgaris (causing urinary tract infections).The incidence of infections caused by these bacteria and others showsigns of increasing incidence in recent years. In 2003, epidemiologistsreported that 5 to 10 percent of patients admitted to hospitals acquirean infection during their stay and that the risk for a hospital-acquiredinfection has risen steadily in recent decades. In November 2004, theCenters for Disease Control and Prevention (CDC) reported an increasingnumber of Acinetobacter baumannii bloodstream infections in patients atmilitary medical facilities treating service members from Afghanistanand the Iraq/Kuwait region.

There exists a need to identify new and effective antibiotic compounds.Antibiotic therapies generally disrupt processes that are unique tobacteria, such as the enzymes and components of the cell wall and theprokaryote ribosomes. The efficacy and safety of antibiotics depend uponthe inhibition of biochemical systems that are unique to bacteria, andthat can be safely inhibited without producing detrimental or undesiredside effects in the individual receiving the antibiotic therapy. Asbacteria become increasingly resistant to existing therapies, it hasbecome difficult to identify unique biochemical pathways that may beinhibited in bacteria that are not also present in the cells of thepatients to be treated.

The biogenesis of cytochrome c in bacteria is a pathway that is apromising target for antibiotic therapy. Cytochrome c is an electrontransport protein that is essential for most aerobic and anaerobicrespiratory chains, as well as other cellular processes such asphotosynthesis and apoptosis. Although three different cytochrome cbiogenesis pathways have been identified in various organisms, two ofthese pathways are unique to bacteria and plants, and only the lastremaining biogenesis pathway is unique to vertebrates, invertebrates,fungus, and some protozoa. Further, cytochrome c is synthesized on theoutside of the cytoplasmic membrane of the bacteria cell, making thebiogenesis of cytochrome c particularly amenable to inhibition by smallmolecules or proteins.

Antibiotic drug discovery is generally a random and laborious process ofbiological screening of compounds against a panel of known bacteriaproteins. The process of antibiotic drug discovery would be greatlyfacilitated by a method of screening that directly measures the effectsof a compound on its target protein in vivo. Further, optimizing thisscreening method to achieve a high-throughput screening method wouldgreatly facilitate the process of developing new and effectiveantibiotics to expand the dwindling arsenal of existing antibiotics.

SUMMARY

Among the several aspects of the invention is provided a method foridentifying a compound that inhibits cytochrome c synthesis in abacterial cell. The method generally comprises contacting the compoundwith a transfected bacterial cell and measuring the amount of cytochromec synthesized using a transfected reporter protein for cytochrome c.

Other aspects and features of the invention are described in more detailbelow.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1. Working models of the three pathways for cytochrome cbiogenesis. Representative organisms that possess each system are listedbelow.

FIG. 2. Plasmids with A) cytochrome c reporters and B) cytochrome cbiogenesis genes.

FIG. 3. Heme stain of arabinose inducible cytochrome c₄ reporters. E.coli strain MG 1655 containing pRGK332 (lanes 1-5) or pRGK331 (lanes6-10) were grown in LB and induced for 3 hours with increasingconcentrations of arabinose, as indicated. Periplasmic shock proteins(50 mg) were separated by SDS-PAGE and stained for heme. The arrowlabeled c4:Pho indicates the cytochrome c₄:alkaline phosphatase fusionprotein. The arrow labeled with c4:His indicates the cytochromec₄hexahistidine tagged di-heme protein.

FIG. 4. Heme stains of periplasmic shock proteins from the indicated E.coli strains with and without recombinant system I or system II. A)Wild-type MG1655 (lanes 1-3) or RKIO3 (lanes 4-10) strains of E. coliwere grown aerobically and induced with 1 mM IPTG and 0.2% arabinose.Above each lane number, c4:Pho indicates the presence of pRGK331; c4:Hisof pRGK332; SysI, pRGK333. B) RKIO3 with the indicated plasmids withsymbols same as in “A” and where SysII refers to pRGK334.

FIG. 5. Reduced and oxidized absorption spectra and mass spectrometryanalysis of holocytochrome c₄:His produced by recombinant biogenesissystems. A) Reduced and oxidized absorption spectra of holocytochromec₄:His from RKIO3 with pRGK332 and pRGK333 (system I). B) Reduced andoxidized absorption spectra of holocytochrome c₄:His from RKIO3 withpRGK332 and pRGK334 (system II). C) ESI-MS analysis of holocytochromec₄:His from RKIO3 with pRGK332 and pRGK333. D) Amino acid sequence ofthe B. pertussis cytochrome c₄:His (SEQ ID NO:21). The signal sequenceis underlined and the CXXCH heme binding sites are in bold. Minor,proteolytic cleavage sites are denoted with linked arrows (see text).

FIG. 6. Western blots and heme stains indicating the stabilization ofholocytochrome c₄ when heme is attached by the system I and II pathways.(A, B) Western blots of periplasmic shock proteins from the indicated E.coli strains. Designations (above lane numbers) are as described in FIG.4. A) Antisera to alkaline phosphatase. B) Cytochrome c₄ antiseraimmunoblotted against the same extracts as in (A). C) The cytochrome c₄hexahistidine tagged proteins from the indicated strains were purifiedover an affinity column and stained for heme or in (D) immunoblottedwith cytochrome c₄ antisera. For panels C and D, the di-hemeholocytochrome c₄ and endogenously proteolyzed 12 kDa holocytochrome C₄proteins are cartooned on the right, as described in the text.

FIG. 7. Cytochrome c₄ synthesis by system I and inhibition withN-methylprotoporphyrin. RKI 03 cultures containing pRGK333 and pRGK332were grown and then IPTG and NMPP were added to induce the synthesis ofsystem I proteins and inhibit heme biosynthesis, respectively. One hourlater, the cytochrome c₄:His reporter was induced with arabinose forthree hours. A) Representative heme stain of soluble B-Per proteinextracts from above cultures. B) Quantification of heme stain intensity(in arbitrary units) with respect to NMPP concentration (average of 3trials, error bars represent standard error).

FIG. 8. Cytochrome c₄ synthesis by system and inhibition withN-methylprotoporphyrin. A) RKIO3 cultures containing pRGK334 and pRGK332were grown and then IPTG and NMPP were added to induce the synthesis ofsystem II proteins and inhibit heme biosynthesis, respectively. One hourlater, the cytochrome c₄:His reporter was induced with arabinose forthree hours. A) Representative heme stain of soluble B-Per proteinextracts from above cultures. B) Quantification of heme stain intensity(in arbitrary units) with respect to NMPP concentration (average of 4trials, error bars represent standard error).

FIG. 9. Holo-CcmE in the recombinant system I as a heme reservoir. A)Western blot using CcmE antisera of membrane proteins from IPTG inducedand uninduced RK 103 cultures with the indicated plasmids. B) Heme stainof membrane proteins separated by SDS PAGE from uninduced RKIO3expressing pRGK333. (20 mg membrane protein loaded per lane.)

FIG. 10. Arabinose-induciblity of cytochrome c₄:His/CemE and inhibitionwith N-methylprotoporphyrin. (A-D) Cultures of RKIO3 containing pRGK345and pRGK349 were grown and then IPTG was added to induce the synthesisof all system I proteins, except CcmE, and arabinose was added to inducethe synthesis of cytochrome c₄:His and CcmE. A) Heme stain ofholocytochrome c₄:His without and with arabinose. 20 mg of B-per extractloaded per lane. B) Western blot using CcmE antisera of same membrane asin (A). C) Representative heme stain of Ni2+ affinity purifiedholocytochrome c₄:His from RKIO3 cultures containing pRGK34S and pRGK349performed as described in FIG. 7 legend. D) Quantification of hemestainable intensity (in arbitrary units) with respect to NMPPconcentration (average of 2 trials).

FIG. 11. Diagram of the current working model for c-type cytochromesbiogenesis from systems I and II. Also shown are models for the HPEXsystem (ChuA) heme porin pathway used in this study and for the firstdedicated step in heme biosynthesis. (^) denotes potential targets forinhibitors used in the current study.

FIG. 12. Heme stains of cytochrome c₄ with increasing concentrations ofALA. E. coli DccmDhemA containing pRGK333 (Lanes 1-5) or pRGK334 (Lanes6-10) were diluted into fresh LB broth without ALA, depletingintracellular ALA. ALA was added (concentrations in mM abovecorresponding lane number) along with 1 mM IPTG for one hour. Thecytochrome c₄:6×His was induced with 0.2% arabinose for three hours andsoluble B-PER protein extracts were prepared. Above each panel pSysIindicates pRGK333, pSysII indicates pRGK334, and c4:6xHis indicatespRGK332.

FIG. 13. Growth of E. coli DccmDhemA with exogenous heme. Overnightcultures of E. coli DccmDhemA or containing pHPEX2 and (A) pRGK333 or(B) pRGK334 were diluted into LB broth without ALA or heme. The cultureswere incubated aerobically at 37° C. for two and one-half hours toexhaust the cultures for ALA. Heme was added at the indicatedconcentrations when noted and growth (A600) was measured. For reference,the growth of E. coli Dccm (wild-type) containing either pRGK333 orpRGK334 is shown (t).

FIG. 14. Exogenous heme acquisition profiles for system I and system II.An E. coli heme auxotroph (RK105) containing pRGK333 or pRGK334,pRGK332, and pHPEX2 (outer membrane heme porin) were grown in theabsence of ALA to exhaust intracellular ALA levels (therefore limitingheme to exogenously added heme). Exogenous heme was added to the culturemedia after 2.5 hours (0 to 10 mM for system 1 and 0 to 100 mM forsystem II) prior to induction of cytochrome c₄:6×His (0.2% arabinose).Holocytochrome C4 was purified from B-PER extracted protein via nickelaffinity chromatography, and separated via SDS-PAGE. Heme stains ofholocytochrome c₄ from representative trials with system I (A) andsystem II (C). Curve fits to average heme stain intensity as apercentage of maximum signal intensity with respect to hemeconcentration is shown in (B) for system I (n=4) and (D) for system II(n=3).

FIG. 15. Heme stain of holocytochrome c₄:6×His with increasingconcentrations of ZnPPIX. E. coli DccmDhemA (RK105) containing pRGK333,pRGK332, and pHPEX2 were grown in 8 mM heme (Lanes 1, 3-5) or 25 mM heme(Lane 2) to an OD600 of approximately 0.5. ZnPPIX was added (Lanes 3-5)and 1 mM IPTG to induce synthesis of the system I proteins. Incubationcontinued for one hour and 0.2% arabinose was added for three hours toinduce the synthesis of the cytochrome c4. The concentrations (in mM) ofheme and ZnPPIX are given above each lane. Above the panel pSysI ispRGK333 and pc4:6xHis is pRGK332.

FIG. 16. Heme stains and western blots for detection of holocytochromec₄ synthesis. E. coli Dccm, containing either (A) pRGK333, pRGK332, andpHPEX2 or (B) pRGK348 and pRGK332, were grown and 1 mM IPTG and ZnPPIXwere added and growth continued for one hour. The cytochrome c₄:6×Hiswas induced with 0.2% arabinose for three hours and soluble B-PERprotein extracts were prepared. The concentrations (in mM) of ZnPPIX aregiven above each lane. Above the panel pSysI is pRGK333, pSysII-chuA ispRGK348, pc4:6xHis is pRGK332 and Dccm is E. coli Dccm.

FIG. 17. Reduced-oxidized absorption spectra and ESI-MS analysis ofcytochrome c₄. Overnight cultures of E. coli Dccm containing pRGK333,pRGK332, and pHPEX2 were diluted into fresh LB broth and grown tomid-log phase. ZnPPIX (8 mM) and IPTG (1 mM) were added and incubationcontinued for an additional hour. Arabinose (0.2%) was added for threehours to induce synthesis of cytochrome c₄:6×His and soluble B-PERextracts were prepared. (A) Reduced (sodium hydrosulphite) and oxidized(ammonium persulfate) absorption spectra and (B) ESI-MS analysis.

FIG. 18. Holocytochrome c₄ synthesis in the presence of ZnPPIX and NMPP.Overnight cultures of E. coli Dccm containing pRGK333, pRGK332, andpHPEX2 were diluted into fresh LB broth and grown to mid-log phase. NMPP(60 mM and 100 mM) and IPTG (1 mM) was added to separate cultures andincubation continued for 30 minutes. ZnPPIX (5 mM and 12.5 mM) was thenadded and incubation continued for an additional 30 minutes. Arabinose(0.2%) was added for three hours to induce synthesis of cytochromec₄:6×His. Independent (NMPP and ZnPPIX) inhibition experiments were alsoperformed. Holocytochrome c4 quantitation by heme stains intensity (inarbitrary units) from three independent trials.

FIG. 19. Growth of E. coli DccmDhemA (RK 104) on ALA. Overnight culturesof E. coli DccmDhemA containing (A) pRGK333 (system I) or (B) pRGK334(system II) were diluted into LB broth without ALA. The cultures weregrown for two and one-half hours at 37° C. with aeration and ALA wasadded (time=0) at the indicated concentrations, with growth (A600)measured at OD600.

FIG. 20. Heme stain (lanes 1-6) and Western blot (lanes 7-12) indicatingSnPPIX inhibits system II holocytochrome c₄:6×His synthesis and is notincorporated into cytochrome c₄ by system II. E. Coli Dccm, containingeither (A) pRGK333, pRGK332, and pHPEX2 or (B) pRGK348 and pRGK332 weregrown and 1 mM IPTG and SnPPIX were added and growth continued for onehour. The cytochrome c₄:6×His was induced with 0.2% arabinose for threehours and soluble B-PER protein extracts were prepared. Theconcentrations (in mM) of SnPPIX are given above each lane. Above thepanel pSysII-chuA is pRGK248, pc4:His is pRGK332 and Dccm is E. ColiDccm.

FIG. 21. Growth of E. Coli Dccm containing pRGK333, pRGK332, and HPEX2in the presence of ZnPPIX. Overnight cultures of E. Coli Dccm containingpRGK333 (system I), pRGK332 (cytochrome c₄:6×His), and pHPEX2 werediluted into fresh LB broth containing the indicated ZnPPIX (in mM)concentrations for growth measurements.

FIG. 22. Western blot (A: lanes 1-7) and heme stain (B: lanes 1-5)indicating ZnPPIX competes with heme. Overnight cultures of E. Coli Dccmcontaining pRGK333, pRGK331, and pHPEX2 were diluted into fresh LB brothcontaining 12.5 mM ZnPPIX and grown to mid-log phase. IPTG (1 mM) wasadded and incubation continued for 30 minutes. Heme was added andincubation continued for 30 minutes. Arabinose (0.2%) was added forthree hours to induce synthesis of cytochrome c₄:PhoA and soluble B-PERprotein extracts were prepared. The concentrations (in mM) of ZnPPIX andheme are given above each lane. Above the panel psysI is pRGK333,pc4:PhoA is cytochrome c₄:PhoA, and Dccm is E. Coli Dcam.

FIG. 23 96 well screen using whole E. Coli cells induced with arabinoseand pipetted into white microtiter plates (rows 1-9). ECL reagent (100μl of Pierce ELISA femto) was injected, plate shaken for 1 minute,incubated for 4 minutes at room temperature, then relative luminescentunits (RLU) were read for 10 sec/well in a Luminoscan (Thermo). (RLUswere stable for at least 20 minutes; a 2 sec/well read yielded similarresults. No false positives or negatives were observed in this trial.Rows A-H in each of the columns 1-10 represent replicates of theexperimental conditions for each respective column. Column 11, rows A-Hcontain decreasing amounts of pure cytochrome c₄ with row A, 2.1 ng; B,1.1 ng; C, 0.6 ng; D, 0.2 ng, and E-H, <0.2 ng. Rows A-H in column 12contain replicates of the experimental conditions for each respectivecolumn.

FIG. 24. Evidence that the ECL signal from whole cells was emanatingfrom the cytochrome C₄. LB cultures of the indicated strains andconditions were sonicated and extracts (15 ml) were separated in anative polyacrylamide gel, and ECL-heme stained. The cytochrome c₄ runsat 50 KDalton in these gels, consistent with the fact that it has beencrystallized as the dimer.

DETAILED DESCRIPTION

A method for identifying a compound that inhibits the synthesis ofcytochrome c in bacteria is provided herein. In general, cytochrome cproteins are essential proteins that function as electron carriers inrespiration in nearly all cells (and photosynthesis in some cells).Cytochrome c proteins function outside the cytoplasmic membrane inprokaryotes, in the intermembrane space of mitochondria, and in thelumen of chloroplasts. C-type cytochromes are generally characterized bya covalent attachment of heme (iron protoporphyrin IX) to the apoproteinvia thioether bonds. Three distinct pathways exist for the synthesis ofcytochrome c (FIG. 1). System I is found primarily in alphaproteobacteria and gamma proteobacteria; system II operates mainly inGram-positive bacteria, beta proteobacteria, epsilon proteobacteria, andplant chloroplasts; and system III is limited to the mitochondria ofcertain eukaryotes. System I has eight or nine proteins, called the Ccmproteins; system II has four proteins, the Ccs proteins, and system IIIconsists of a single protein. Generally, the function of most of theproteins of the system I and II pathways is to help shuttle heme throughthe cytoplasmic membrane or help link heme to the cytochrome capoprotein. Compounds that inhibit the synthesis of cytochrome c may beeffective antibiotic agents.

I. Compositions

a) Bacterial Cells

One aspect of the invention provides an engineered bacterial cell inwhich the chromosomal region encoding the system I Ccm proteins isdisrupted or deleted (i.e., Δccm). The nucleotide sequence encoding theCcm proteins is sometimes a contiguous sequence (i.e., the ccm operon inE. coli). As will be appreciated by one skilled in the art, thechromosomal region encoding the Ccm proteins may be disrupted or deletedby a variety of methods. (For example, see Ausubel et al. (2003) CurrentProtocols in Molecular Biology, John Wiley & Sons, New York N.Y., ch.1.) Suitable methods include transposon-mediated mutagenesis, retargetedgroup II introns, insertion of an antibiotic-resistance cassette,site-specific recombination, or a combination thereof. Examples ofsuitable transposons include Tn3, Tn5, Tn9, Tn10, Tn903, Tn1681, Mu, andminiMu. Suitable antibiotic-resistance cassettes includeampicillin-resistance, chloramphenicol-resistance, kanamycin-resistance,spectinomycin-resistance, and tetracycline-resistance cassettes.Suitable examples of site-specific recombination systems include theFlp/FRT system from Schizosaccharomyces cerevisiae, the Cre/loxP systemfrom E. Coli bacteriophage P1, the R/RS system from Zygosaccharomycesrouxii, the φC31/attB,attP system from Streptomyces phage phiC31, andthe mutant Gin/gix system from enteric bacteriophage Mu. In a preferredembodiment, the nucleotide sequence encoding the Ccm proteins may bedeleted and replaced with an antibiotic-resistance cassette usingPCR-based techniques well known in the art (and detailed in theexamples).

The bacterial cell may further comprise a deletion of the chromosomalregion encoding the HemA protein (i.e., ΔhemA). HemA is an aminolevulinic acid (ALA) synthetase, which is the first enzyme in the hemebiosynthesis pathway. The nucleotide sequence encoding HemA may bedisrupted or deleted using any of the aforementioned methods. It shouldbe noted that other enzymes in the heme biosynthesis pathway may beinactivated by nucleotide sequence deletion or disruption withoutdeparting from the scope of the invention.

The bacterial cell may be an alpha proteobacterial cell or a gammaproteobacterial cell (i.e., a cell containing a system I pathway). Alphaproteobacteria include Caulobacterales (e.g., Caulobacter),Parvularculales, Rhizobiales, Rhodobacterales, Rhodospirillales (e.g.,Acetobacter), Rickettsiales, and Sphingomonadales. Gamma proteobacteriainclude Acidithiobacillales, Aeromonadales (e.g., Aeromonas),Alteromonadales, Cardiobacteriales, Chromatiales, Enterobacteriales(e.g., Escherichia), Legionellales, Methylococcales, Pasteurellales(e.g., Haemophilus), Pseudomonadales (e.g., Pseudomonas), Vibrionales(e.g., Vibrio), and Xanthomonadales. In one embodiment, the bacterialcell may be Bradyrhizobium japonicum in which the nucleotide sequenceencoding the CcmA-H proteins is disrupted or deleted. In anotherembodiment, the bacterial cell may be Paracoccus denitrificans in whichthe nucleotide sequence encoding the CcmA-H proteins is disrupted ordeleted. In yet another embodiment, the bacterial cell may beRhodobacter capsulatus in which the nucleotide sequence encoding theCcmA-H proteins is disrupted or deleted. In still another embodiment,the bacterial cell may be Escherichia Coli in which the nucleotidesequence encoding the CcmA-H proteins is disrupted or deleted. In analternate embodiment, the bacterial cell may be R. capsulatus in whichthe nucleotide sequence encoding the CcmA-H proteins and the nucleotidesequence encoding the HemA protein are deleted (ΔccmΔhemA). In apreferred embodiment, the bacterial cell may be a Δccm E. Coli cell. Inanother embodiment, the bacterial cell may be a ΔccmΔhemA E. Coli cell.One skilled in the art will appreciate that a Δccm bacterial cell cannotsynthesize cytochrome c and a ΔhemA bacterial cell can grow only in thepresence of exogenous ALA.

b) Cytochrome c Pathway Constructs

Another aspect of the invention provides constructs for the delivery andexpression of the cytochrome c biosynthesis enzymes in a Δccm bacterialcell. The construct may comprise a nucleotide sequence encoding the Ccmproteins of system I, or the construct may comprise a nucleotidesequence encoding the Ccs proteins of system II.

The nucleotide sequence encoding Ccm proteins or Ccs proteins may beisolated by PCR amplification or other techniques well known in the art.(See the examples and also Ausubel et al. (2003) Current Protocols inMolecular Biology, John Wiley & Sons, New York N.Y., ch. 3 and 6.). Asnoted in section I (a), the nucleic acid encoding the system I Ccmproteins may be from an alpha proteobacterium or a gammaproteobacterium. In one embodiment, the nucleic acid sequence encodingthe CcmA-H proteins of R. capsulatus may be isolated. In a preferredembodiment, the nucleic acid sequence encoding the CcmA-H proteins of E.coli may be isolated. Although the system II pathway includes fourproteins, it appears that two proteins, CcsA and CcsB, may be may besufficient to restore cytochrome c biosynthesis in a heterologous hostcell. The nucleic acid sequence encoding the Ccs proteins may be from abeta proteobacterium, an epsilon proteobacterium, a Gram-positivebacterium, or a cyanobacterium. Suitable beta proteobacteria includeBurkholderiales (e.g., Bordetella), Hydrogenophilales, Methylophilales,Neisseriales, Nitrosomonadales, Rhodocyclales, and Procabacteriales.Suitable epsilon proteobacteria include Campylobacterales (e.g.,Helicobacter) and Nautiliales. Suitable gram-positive bacteria includeBacillus, Listeria, Enterococcus, Mollicutes, and Mycobacteriumtuberculosis. Suitable cyanobacteria include Synechocystis, Nostoc,Anabaena, and Gloeocapsa. In one embodiment, the nucleic acid sequenceencoding the CcsA and CcsB proteins of Bacillus subtilis may beisolated. In another embodiment, the nucleic acid sequence encoding theCcsA and CcsB proteins of Bordetella pertussis may be isolated. In yetanother embodiment, the nucleic acid sequence encoding the fused CcsBAprotein of Helicobacter species may be isolated. In a preferredembodiment, the nucleic acid sequence encoding the fused CcsBA proteinof H. pylori may be isolated

The isolated nucleic acid is typically cloned into an appropriateexpression vector so that the proteins may be expressed in the bacterialcell from section I (a). An expression vector is typically a vector thatcontains the necessary elements for transcriptional and translationalcontrol of the inserted nucleic acid sequence in the host cell. Thevector may be a plasmid vector, a Lambda bacteriophage vector, aLambda-derived vector, or a filamentous phage-derived vector. In oneembodiment, the vector may be a plasmid. In one embodiment, the vectormay be a pGEX-derived plasmid. In another embodiment, the vector may bea pBAD-derived plasmid.

The nucleotide sequence encoding the Ccm or Ccs proteins is generallyoperably linked to an inducible promoter so that the timing ofexpression may be controlled. Suitable examples of inducible promotersinclude, but are not limited to, those induced by expression of anexogenous protein (e.g., T7 RNA polymerase, SP6 RNA polymerase),presence of a small molecule (e.g., IPTG, arabinose, galactose,tetracycline, steroid hormone, abscisic acid), metals (e.g., copper,zinc, cadmium), and environmental factors (e.g., heat, cold, stress).The type of promoter can and will vary depending upon other constructsthat may be used. In one embodiment, the promoter may be induced byIPTG. Suitable examples of IPTG-inducible promoters include the TAC,lac, lacUV5, and trc promoters. In another embodiment, the promoter maybe induced by arabinose. Suitable arabinose-inducible promoters includearaB, araBAD, and araFG.

The vector typically also comprises a selectable marker, which is asequence that codes for a protein that provides resistance to anantibiotic. Suitable selectable markers include those that provideresistance to ampicillin, carbenacillin, chloramphenicol, kanamycin,spectinomyin, and tetracycline. The choice of selectable marker can andwill vary depending upon other features of the bacterial cell and otherconstructs that may be used. Methods well known to those skilled in theart may be used to construct the expression vectors. (See Ausubel et al.(2003) Current Protocols in Molecular Biology, John Wiley & Sons, NewYork N.Y., ch. 1, 3 and 16).

c) Cytochrome c Reporter Constructs

The invention also provides cytochrome c reporter constructs, whichfacilitate monitoring of the synthesis of cytochrome c in therecombinant cells (i.e., a ΔccmΔhemA or Δccm bacterial cell transfectedwith a Ccm or a Ccs expression vector). Typically, the cytochrome creporter will produce a protein of a different size or differentimmunogenicity than the endogenous cytochrome c of the host bacterialcell. In one embodiment, the cytochrome c protein may be the cytochromec₄ protein of Bordetella pertussis. In another embodiment, thecytochrome c protein may be the cytochrome c₂ protein of R. capsulatus.

Additionally, the reporter protein may be a fusion of the cytochrome cprotein and another protein. Typically the fusion partner protein has avariety of research tools available for its detection or purification.The fusion partner protein may be alkaline phosphatase (AP),glutathione-S-transferase (GST), maltose binding protein (MBP),luciferase, a 6×His tag, a myc tag, or a Flag tag. In one embodiment,the cytochrome c reporter may be a cytochrome c₄:alkaline phosphatasefusion protein. In another embodiment, the cytochrome c reporter may bea cytochrome c₄:6×His fusion protein. In yet another embodiment, thecytochrome c reporter may be a cytochrome c₄:Flag tag fusion protein

In general, the cytochrome c reporter construct will be an expressionvector with an inducible promoter and a selectable marker, as detailedin section I (b) and may be constructed using procedures well known inthe art, as mentioned above.

II. Methods of Screening for a Compound that Inhibits the Synthesis ofCytochrome c in Bacteria

Another aspect of the invention provides methods for identifyingcompounds that inhibit the synthesis of cytochrome c in a bacterialcell. Using the deletion mutant cells described in section I (a) and theexpression constructs described in sections I (b) and (c), compoundshave been and may be identified that inhibit the synthesis of cytochromec. In general, these inhibitors block one of the steps of the system Ior system II cytochrome c synthesis pathways, but will not affect theeukaryotic system III pathway. Furthermore, since cytochrome c synthesisoccurs on the outer surface of the cytoplasmic membrane of bacteria,cytochrome c biosynthesis is a readily accessible target for anantibacterial agent.

The method comprises transfecting a Δccm bacterial cell with aninducible Ccm expression vector (provides system I proteins) or aninducible Ccs expression vector (provides system II proteins), as wellas an inducible cytochrome c reporter vector. In some embodiments, theΔccm bacterial cell may further comprise ΔhemA. A variety of methods aresuitable for introducing an expression vector into a bacterial cell. Thebacterial cell may be transfected with the expression vector by a heatshock. The bacterial cell may be transfected with the expression vectorby high-voltage electroporation. Methods to make bacterial cellscompetent to take up vectors are well known in the art.

The Δccm bacterial cell may further comprise a porphyrin porinexpression vector. Expression of a porin protein may permit passage of ametalloporphyrin, such as heme (iron protoporphyrin IX) through theouter membrane of the bacterial cell. In one embodiment, the porphyrinporin may be ChuA, a heme receptor from Escherichia coli. In anotherembodiment, the porphyrin porin may be a porin from Bartonellaquintanta. It should be noted that porphyrin porins from other bacteriamay be used without departing from the scope of the invention. Oneskilled in the art will appreciate that a Δccm bacterial cell harboringa Ccm or a Ccs expression vector and a porphyrin porin expression vectorwill typically grow only in the presence of exogenous heme.

The method further comprises contacting the aforementioned transfectedbacterial cell with a test compound. “Contacting” typically entailsgrowing the cell in the presence of the compound upon induction of thevarious expression constructs. Methods are well known in the art forgrowing bacterial cells in appropriate culture media under optimalgrowth conditions in the presence of the appropriate antibiotics andother compounds (e.g., ALA, inducers). The timing of induction of thevarious expression constructs can and will vary depending upon thecompound being screened.

The method further comprises determining the amount of cytochrome creporter protein produced in the presence of the compound relative tothe amount of reporter protein produced in the absence of the compound.A decrease in amount of cytochrome c reporter protein is an indicationthat the compound inhibits the synthesis of cytochrome c. The amount ofcytochrome c reporter protein produced by the cell may be measured in anextract of the cell. Alternatively, the cytochrome c reporter proteinmay be partially purified from the cell extract before the amount ismeasured. Various methods are known in the art for purifying proteinsfrom crude cell extracts. A preferred method includes affinitychromatography, in which the fusion partner of cytochrome c is utilizedto capture the entire reporter fusion protein. Typically, a solidsupport medium containing a specific compound is used to bind the fusionpartner of the reporter protein. Suitable examples includeglutathione-linked beads that bind GST, maltose-linked beads that bindMBP, Ni²⁺ beads that bind 6×His tags, anti-Flag antibody-linked beadsthat bind Flag tags, and anti-AP antibody-linked beads that bind AP.

A variety of methods may be used to detect the cytochrome c reporterprotein. The detection method may include gel electrophoresis,immunodetection, heme staining, or a combination thereof. In oneembodiment, the cytochrome c reporter protein may be resolved bySDS-polyacrylamide gel electrophoresis. The polyacrylamide gel may thenbe stained for heme groups using a colorimetric stain, such aso-dianisidine or dimethoxy benzidine. Alternatively, the polyacrylamidegel may be stained for heme groups using a chemiluminescent substrate.The polyacrylamide gel may be blotted and probed with an antibodyagainst a part of the cytochrome c reporter protein. The antibody mayrecognize one or more epitopes of the cytochrome c protein or the fusionpartner protein. As described in section I (c), the fusion partner maybe alkaline phosphatase (AP), glutathione-S-transferase (GST), maltosebinding protein (MBP), luciferase, a 6×His tag, a myc tag, or a Flagtag. In another embodiment, the heme of the cytochrome c reporterprotein may be detected in solution using a chemiluminescent substrate.The emission of chemiluminescent product may be measured using aluminometer. In yet another embodiment, the cytochrome c reporterprotein may be detected using mass spectrometry.

A variety of compounds may be screened using this method. Suitable testcompounds include, but are not limited to, metalloporphyrins. Suitablemetalloporphyrins include zinc protoporphyrin IX, tin protoporphyrin IX,manganese protoporphyrin IX, cobalt protoporphyrin IX, aluminumprotoporphyrin IX, copper protoporphyrin IX, chromium protoporphyrin IX,palladium protoporphyrin IX, platinum protoporphyrin IX, and vanadiumprotoporphyrin IX. The test compound may be N-methylprotoporphyrin or aderivative or analog of N-methylprotoporphyrin. The test compound may bea modified heme that possesses only one of the two vinyl groups, i.e.,the 2-vinyl group or the 4-vinyl group. The test compound may be amodified heme in which the 6-propionate group has been modified. As anexample, the 6-propionate group may be converted to a carboxyamide. Allof the modified heme analogs may possess iron or any of theaforementioned metals.

In a preferred embodiment, the screening method comprises a Δccm E. Colicell transfected with a first expression plasmid encoding the CcmA-Hproteins of E. Coli or the fused CcsBA protein of H. pylori and a secondexpression plasmid encoding cytochrome c reporter protein. Thecytochrome c reporter second plasmid encodes a cytochrome c₄:alkalinephosphatase fusion protein or a cytochrome c₄:6×His fusion protein,wherein the cytochrome c₄ protein is from B. pertussis. The codingregion of the first plasmid is operably linked to an IPTG-induciblepromoter and the coding region of the second plasmid is operably linkedto an arabinose-inducible promoter. The amount of cytochrome c reporterprotein may be measured in cell extracts using a chemiluminescentsubstrate and a luminometer. In general, this system will identifycompounds that inhibit cytochrome c synthesis, as well as compounds thatinhibit heme synthesis. The Δccm E. Coli cell may further comprise aporphyrin porin expression plasmid. The porphyrin porin may be ChuA, aheme receptor from E. Coli. Since the cells of this later system requireexogenous heme, the compounds identified in this system generally willbe inhibitors of cytochrome c synthesis.

III. Kits for Screening for a Compound that Inhibits the Synthesis ofCytochrome c

A further aspect of this invention is the provision of kits foridentifying inhibitors of the synthesis of cytochrome c in bacterialcells. A kit comprises a strain of Δccm E. Coli cells transfected with afirst expression plasmid vector encoding the CcmA-H proteins of E. Colior the fused CcsBA protein of H. pylori and a second expression plasmidencoding a cytochrome c reporter protein. The cytochrome c reporterprotein is either cytochrome c₄:alkaline phosphatase fusion protein or acytochrome c₄:6×His fusion protein, wherein the cytochrome c4 protein isfrom B. pertussis. The coding region of each expression plasmid isoperably linked to an inducible promoter, whereby expression of thefirst plasmid is controlled by IPTG and expression of the second plasmidis controlled by arabinose. The Δccm E. Coli cells of the kit mayfurther comprise an exogenous porphyrin porin. Also provided in the kitsare instructions for growing the cells and for contacting the cells witha compound to be screened. A kit may also comprise means for measuringthe production of the cytochrome c reporter protein produced in theabsence or the presence of a test compound, as described in section II.

IV. Methods of Treatment

The invention also provides a method for treating a subject having abacterial infection. The method comprises administering to the subjectan effective amount of a cytochrome c synthesis inhibitor. In general,the cytochrome c synthesis inhibitors identified using the methods ofthis invention will inhibit the synthesis of cytochrome c in bacterialcells, but will not affect the synthesis of cytochrome c in eukaryoticcells.

Bacterial cells in which the synthesis of cytochrome c may be inhibitedinclude any organism with a system I pathway (e.g., alpha and gammaproteobacteria) or a system II pathway (e.g., beta and epsilonproteobacteria and most Gram-positive bacteria). In particular, bacteriathat may be inhibited include Bacteroides species, Bartonella species,Brucella species, Camphylobacter species, Haemophilus species,Helicobacter species, Mycobacterium tuberculosis, Neisseria species,Porphyromonas species, Pseudomonas aeruginosa, Rickettsiae species,Salmonella species, Vibrio species, and Yersinia species. Diseasescaused by these bacteria include tuberculosis, nosocomial diseases,rickettsiae diseases, ulcers, food poisonings, abcesses, sinusitis, andcystic fibrosis (via Pseudomonas aeruginosa).

Non-limiting examples of subjects that may be treated with a c synthesisinhibitor include humans, primates, cats, dogs, cattle, swine, poultry,sheep, horses, fish, research animals, and zoo animals.

The chemical nature of the cytochrome c synthesis inhibitor can and willvary. In one embodiment, the cytochrome c synthesis inhibitor may beN-methylprotoporphyrin.

In another embodiment, the cytochrome c synthesis inhibitor may be zincprotoporphyrin IX. In still another embodiment, the cytochrome csynthesis inhibitor may be tin protoporphyrin IX.

The cytochrome c synthesis inhibitor may be formulated intopharmaceutical compositions and administered by a number of differentmeans that will deliver a therapeutically effective dose. Suchcompositions may be administered orally, parenterally, by inhalationspray, rectally, intradermally, transdermally, or topically in dosageunit formulations containing conventional nontoxic pharmaceuticallyacceptable carriers, adjuvants, and vehicles as desired. Topicaladministration may also involve the use of transdermal administrationsuch as transdermal patches or iontophoresis devices. The termparenteral as used herein includes subcutaneous, intravenous,intramuscular, or intrasternal injection, or infusion techniques.Formulation of drugs is discussed in, for example, Hoover, John E.,Remington's Pharmaceutical Sciences, Mack Publishing Co., Easton, Pa.(1975), and Liberman, H. A. and Lachman, L., Eds., Pharmaceutical DosageForms, Marcel Decker, New York, N.Y. (1980).

Injectable preparations, for example, sterile injectable aqueous oroleaginous suspensions, may be formulated according to the known artusing suitable dispersing or wetting agents and suspending agents. Thesterile injectable preparation may also be a sterile injectable solutionor suspension in a nontoxic parenterally acceptable diluent or solvent.Among the acceptable vehicles and solvents that may be employed arewater, Ringer's solution, and isotonic sodium chloride solution. Inaddition, sterile, fixed oils are conventionally employed as a solventor suspending medium. For this purpose, any bland fixed oil may beemployed, including synthetic mono- or diglycerides. In addition, fattyacids such as oleic acid are useful in the preparation of injectables.Dimethyl acetamide, surfactants including ionic and non-ionicdetergents, and polyethylene glycols may be used. Mixtures of solventsand wetting agents such as those discussed above are also useful.

Solid dosage forms for oral administration may include capsules,tablets, pills, powders, and granules. In such solid dosage forms, thecompound is ordinarily combined with one or more adjuvants appropriateto the indicated route of administration. If administered per os, thecompound may be admixed with lactose, sucrose, starch powder, celluloseesters of alkanoic acids, cellulose alkyl esters, talc, stearic acid,magnesium stearate, magnesium oxide, sodium and calcium salts ofphosphoric and sulfuric acids, gelatin, acacia gum, sodium alginate,polyvinylpyrrolidone, and/or polyvinyl alcohol, and then tableted orencapsulated for convenient administration. Such capsules or tablets maycontain a controlled-release formulation as can be provided in adispersion of active compound in hydroxypropylmethyl cellulose. In thecase of capsules, tablets, and pills, the dosage forms may also comprisebuffering agents such as sodium citrate, or magnesium or calciumcarbonate or bicarbonate. Tablets and pills can additionally be preparedwith enteric coatings.

For therapeutic purposes, formulations for parenteral administration maybe in the form of aqueous or non-aqueous isotonic sterile injectionsolutions or suspensions. These solutions and suspensions may beprepared from sterile powders or granules having one or more of thecarriers or diluents mentioned for use in the formulations for oraladministration. The compounds may be dissolved in water, polyethyleneglycol, propylene glycol, ethanol, corn oil, cottonseed oil, peanut oil,sesame oil, benzyl alcohol, sodium chloride, and/or various buffers.Other adjuvants and modes of administration are well and widely known inthe pharmaceutical art.

Liquid dosage forms for oral administration may include pharmaceuticallyacceptable emulsions, solutions, suspensions, syrups, and elixirscontaining inert diluents commonly used in the art, such as water. Suchcompositions may also comprise adjuvants, such as wetting agents,emulsifying and suspending agents, and sweetening, flavoring, andperfuming agents.

The amount of the cytochrome c synthesis inhibitor that is combined withthe carrier materials to produce a single dosage of the composition canand will vary depending upon the patient and the particular mode ofadministration. Those skilled in the art will appreciate that dosagesmay also be determined with guidance from Goodman & Goldman's ThePharmacological Basis of Therapeutics, Ninth Edition (1996), AppendixII, pp. 1707-1711 and from Goodman & Goldman's The Pharmacological Basisof Therapeutics, Tenth Edition (2001), Appendix II, pp. 475-493.

DEFINITIONS

The term “heme” as used herein refers to a prosthetic group comprisingan iron atom in the center of a large organic cyclic macromoleculecalled porphyrin. Specifically, the heme mentioned herein is a c-typeheme, which is found in c-type cytochromes.

The term “metalloporphyrin” as used herein refers to a compound formedby the combination of a porphyrin with a suitable metal.

The term “porin” a used herein refers to a large transmembrane proteinthat forms a pore in a membrane through which small molecules may pass.

The term “protoporphyrin” or “protoporphyrin IX” as used herein refersto a mature porphyrin ring that has not complexed with a metal atom.

The terms “transfect” or “transfection” as used herein refers to theprocess during which a cell allows entry of nucleic acid molecules,which do not integrate in the host chromosome, but rather remainextrachromosomal.

As various changes could be made in the above constructs and methodswithout departing from the scope of the invention, it is intended thatall matter contained in the above description and in the examples givenbelow, shall be interpreted as illustrative and not in a limiting sense.

EXAMPLES

The following examples detail various iterations of the invention.

Cytochromes c proteins are electron transport proteins that areessential for aerobic and anaerobic respiration, as well as many othercellular processes, such as photosynthesis and apoptosis. Cytochromes care distinguished from other cytochromes by a covalent ligation of theheme vinyl groups to the cysteine residues of apocytochrome c in a CXXCHmotif, and are ubiquitous among all life.

Three distinct pathways for the synthesis of c-type cytochromes, calledsystem I, II and III have been identified for various organisms. SystemsI and II deliver heme to the site of assembly, maintain theapocytochrome c in a reduced state, and facilitate an energyindependent, covalent ligation of the heme to the apocytochrome c. Thesystem I pathway, which uses eight proteins encoded by the ccm genes, isfound in α and γ proteobacteria, archaea, and plant mitochondria. Thesystem II pathway, comprised of four proteins, is used by Gram-positivebacteria, β and ε proteobacteria, plant chloroplasts, and cyanobacteria.Four genes, called ccsB, ccsA, ccsX and dsbD (or its homologue ccdA) areinvolved in the system II pathway, but CcsB and CcsA proteins may be allthat are necessary, other than a general thiol reductant, for thesynthesis of c-type cytochromes via system II. Eukaryotes (yeast,invertebrates and vertebrates) utilize the system III pathway, comprisedof a single soluble enzyme called cytochrome c heme lyase (CCHL), foundin the mitochondria.

In the examples below, a heterologous recombinant approach inEscherichia Coli was employed. In Example 1, a cytochrome c reporter wasengineered and inserted into E. Coli. All cytochrome c biogenesis geneswere excised out of E. Coli and complemented by engineered system I orsystem II genes in Example 2. This recombinant E. Coli strain was usedin Example 3 to compare the ability of system I and system II to deliverheme to the cytochrome c biosynthetic pathways. Example 4 furtherexamined the heme delivery capability of system I by discovering thepresence of a heme storage pool within the system I pathway proteins.The affinity for heme in systems I and II was compared in Example 5.Example 6 compared the ability of system I and II to utilize othernon-ferrous metals such as copper, zinc, tin and manganese in thebiogenesis of cytochromes c. Recombinant E. Coli was further used todiscover and characterize the inhibitory properties of metalloporphyrinZnPPIX on systems I and II cytochromes c biogenesis in Example 7. InExample 8, the techniques developed for the recombinant E. Coli strainmay be optimized for microtiter plates to develop a method of highthroughput screening for cytochrome c inhibitors.

Materials and Methods for Examples 1-8

a) Bacterial Growth Conditions

All E. Coli strains were grown aerobically at 37° C. in Luria-Bertanimedia (LB; Difco) with shaking at 300 rpm at 37° C. Antibiotics(Sigma-Aldrich; St. Louis, Mo.) were used at the followingconcentrations: carbenicillin 50 μg mL⁻¹, tetracycline 15 μg mL⁻¹,chloramphenicol 20 μg mL⁻¹, kanamycin 100 μg mL⁻¹, and ampicillin 100 μgmL⁻¹. Aminolevulinic acid (ALA; Sigma-Aldrich) was used at aconcentration of 50 μg mL⁻¹ (300 μM), unless otherwise noted.Metalloporphyrins zinc (II) protoporphyrin IX (ZnPPIX), tin (IV)protoporphyrin IX (SnPPIX), manganese (III) protoporphyrin IX (MnPPIX),and cobalt (III) protoporphyrin IX (CoPPIX) were obtained from FrontierScientific (Logan, Utah) and were dissolved in 0.1 N NaOH to 10 mg mL⁻¹stock concentration. Hemin (heme; Frontier Scientific) was dissolved in50% DMSO to 10 mg mL⁻¹ stock concentration.

b) Construction of RK103

A derivative of E. coli MG1655 with the eight ccm genes replaced by akanamycin-resistance cassette (Δccm) was constructed by the procedure ofWanner and colleagues (Datsenko and Wanner, 2000). Polymerase chainreaction (PCR) products were generated by using a pair of primers,Δccm-left and Δccm-right, and a template plasmid, pKD4, bearing akanamycin-resistance marker flanked by FLP recombinase target sites. Alloligonucleotide primers used are shown in Table 1. The oligonucleotidesinclude sequences identical to the C-terminal coding sequence of ccmHand the N-terminal coding sequence of ccmA, respectively, for targetingrecombination events to the corresponding loci in the E. colichromosome. The 3′ end of the oligonucleotides incorporate the pKD4priming sites P1 and P2 respectively. The PCR product was introducedinto MG1655 cells expressing the phage A Red recombinase encoded onpKD46. Transformants were selected on LB-kanamycin at 37° C. Severalcolonies that were resistant to kanamycin but sensitive to ampicillin(indicating a loss of pKD46) were screened by PCR with test primersflanking the recombination site to identify strains with a deletion atthe locus.

c) Construction of E. coli Strain RK105

A derivative of the E. coli Δccm (RK103, see above) with the hemA genereplaced with a kanamycin resistance cassette was constructed by theprocedure of Datsenko and Wanner (2000). PCR products were generatedusing a template plasmid, pKD4, containing a kanamycin resistancecassette that is flanked by FLP recombinase target sites, and a pair ofoligonucleotide primers, ΔhemA-left and ΔhemA-right (see Table 1). Theoligonucleotide primers included sequences identical to the N-terminaland C-terminal coding sequence, respectively, of hemA, for targetingrecombination events to the corresponding loci in the E. colichromosome. The 3′ end of the oligonucleotides also incorporated thepKD4 priming sites P1 and P2, respectively. The PCR product wasintroduced into E. coli Δccm (RK 104), cured for kanamycin resistance,expressing the λ phage Red recombinase encoded on pKD46. Transformantswere selected on LB with kanamycin and ALA at 37° C. Several coloniesthat were resistant to kanamycin but sensitive to ampicillin (indicatinga loss of pKD46) were screened by PCR with oligonucleotide primersflanking the recombination site to identify strains with a deletion ofthe hemA gene.

d) Constructions of Plasmids

Escherichia coli strain TB1 was used as host for all clonings. pGex-4T-1(Amersham Biosciences; Piscataway, N.J.) derived vectors have anN-terminal GST fusion to the insert under the control of theIPTG-inducible Tac promoter. All oligonucleotide primers used are shownin Table 1.

pRGK333 (system I plasmid, containing all eight ccmA-ccmH genes) wasconstructed by amplifying the entire 6.3 kb ccm locus by PCR with theoligonucleotides SysI-Nterm and SysI-Cterm. The amplified product wasdigested and ligated into the vector, pGEX-4T-1 digested with BamHI andEcoRI.

pRGK345 (ΔccmE), containing an in frame deletion of ccmE, was generatedin a two step process that takes advantage of the overlapping stop andstart codons between ccmD and ccmE, and between ccmE and ccmF. Thecoding region of ccmABCD was amplified by PCR with the oligonucleotidesSysI-Nterm and CcmD-Cterm. The amplified product was digested andligated into the vector, pGEX-4T-1 digested with BamHI and EcoRI. Theresulting intermediate plasmid pRGK344 (pGexccmABCD) encodes CcmABCDwith an N-terminal fusion to GST. Second, ccmFGH was amplified by PCRwith the oligonucleotides CcmF-Nterm and SysI-Cterm. The amplifiedproduct was digested and ligated into the vector, pGexccmABCD digestedwith NdeI and EcoRI.

pRGK346 (ΔccmH), containing an in frame deletion of ccmH, was generatedby amplifying the coding region of ccmABCDEFG by PCR with theoligonucleotides SysI-Nterm and CcmG-Cterm. The amplified product wasdigested and ligated into the vector, pGEX-4T-1 digested with BamHI andEcoRI.

For construction of an arabinose-inducible, chloramphenicol-resistantvector, pBAD24 (Khlebnikov et al., 2000) was used as a template with theoligonucleotides pBad24-left and pBad24-right. The amplified product wascut with HinDIII and ligated with the chloramphenicol-resistancecassette cut from pHP45 ΩCmr (Alexeyev et al., 1995) using HinDIII togenerate pRGK330 (with Cmr). The cycC:phoA fusion gene was PCR amplifiedusing pRGK323 (Beckett et al., 2000) as a template with theoligonucleotides c₄-pho-Nterm and c₄-pho-Cterm. The amplified reportercassette was digested with NheI and Acc651 and ligated into the pRGK330multiple cloning site to generate pRGK331 (c₄:Pho).

For construction of a cytochrome c₄:hexahistidine reporter, the B.pertussis cycC gene was PCR amplified from pRGK323 with theoligonucleotides c₄-pho-Nterm and c₄-6×His-Cterm to add a C-terminal6×His tag to the reporter. The amplified product was digested with NheIand Acc651 and ligated into pRGK330 to generate pRGK332(c₄:His).

For construction of a plasmid expressing system II, the H. pylori ccsBAcoding region was PCR amplified from genomic DNA with theoligonucleotides SysII-Nterm and SysII-Cterm. The amplified product wasdigested with BamHI and EcoRI and ligated into pGEX-4T-1 to generatepRGK334 (system II plasmid).

For construction of a cytochrome c₄:hexahistidine reporter containing anarabinose-inducible ccmE gene with a C-terminal 6×His tag, the E. coliccmE gene was amplified from pRGK333 with oligonucleotides CcmE*-Ntermand CcmE*-Cterm. The amplified product was cut with KpnI and PstI andligated into pRGK332 to generate pRGK349.

For the construction of pRGK348, it was necessary to correct for theapparent instability of pRGK334 (system II) when both pRGK332 (c₄:6×His)and pHPEX2 (Varnado and Goodwin, 2004) are present, by inserting thechuA gene from pHPEX2 downstream of the ccsBA gene in pRGK334. The chuAgene along with the lacUV5 promoter, ribosome binding site, and the chuAstop codon were cut out of pHPEX2 using XbaI. Following agarose gelpurification (Gene Clean, BIO 101 Systems, Irvine, Calif.) of anapproximately 3.6 kb restriction fragment, the XbaI ends were filled inwith Klenow fragment of E. coli DNA polymerase I and ligated to Tth111Idigested pRGK334. The resulting plasmid (pRGK348) contains the chuA geneinserted 210 bp downstream of the ccsBA stop codon. The expression ofchuA from pRGK348 was verified by growth of E. coli ΔccmΔhemA (RK105) inLB supplemented with heme.

e) Production of Antibodies to B. pertussis Cytochrome c₄

For overexpression of the soluble cytochrome c₄ protein, encoded by theB. pertussis cycC gene, pRGK332 was coexpressed with pRGK333 in the E.coli TB1 strain. Cells were grown to mid-exponential phase (A600=0.6) inLB containing ampicillin and chloramphenicol and induced with IPTG (1mM) and arabinose (0.2%) for 3 h. The cytochrome c₄ protein was purifiedusing Ni²⁺-chelating resin (Novagen) as previously described (Feissneret al., 2005). Antiserum was generated in New Zealand white rabbits at acommercial facility (Cocalico Biologicals; Reamstown, Pa.). Theantibodies were purified from the serum by ammonium sulphateprecipitation and used at a 1:6000 dilution for Western blot.

f) Production of Antibodies to E. coli CcmE

For overexpression of the E. coli CcmE protein, the soluble,134-amino-acid periplasmic region (called CcmE*) was amplified by PCRusing MG1655 genomic DNA as a template and the oligonucleotidesCcmE*-Nterm and CcmE*-Cterm. The resulting amplified product wasdigested with NcoI and XhoI and cloned into the plasmid pET2-Blue(Novagen; Madison, Wis.) to create the plasmid pRGK347. The CcmE*periplasmic protein containing a C-terminal 6×His tag was overexpressedfrom pRGK347 in the Tuner pLacI strain of E. coli (Novagen). Cells weregrown to mid-exponential phase (A600=0.6) in LB containing carbenacillinand induced with IPTG (1 mM) for 3 h. Cells were harvested, washed in 20mM Tris (pH 8) and resuspended in lysis buffer [20 mM Tris pH 8,lysozyme (1 mg ml-1), Triton X-100 (1%)]. After incubation on ice for 20min, bacteria were lysed by sonication (twice for 3 min each, BransonModel 200) using a microtip at a power setting of 40% and a duty cycleof 50%. Debris was removed by centrifugation (10 000 g, 15 min, 4° C.)and the 6×His-tagged CcmE* was purified by chromatography overNi²⁺-chelating affinity resin. Eluted protein was concentrated withCentricon 10 columns (Millipore; Billerica, Mass.) and dialysed againststorage buffer (20 mM Tris pH 8, 200 mM NaCl) to remove the imidazole.Purity of the preparations, as assessed using SDS-PAGE and staining withCoomassie brilliant blue, was greater than 95%. Antiserum was generatedin New Zealand white rabbits at a commercial facility (CocalicoBiologicals). The antibodies were purified from the serum by ammoniumsulphate precipitation and used at a 1:5000 dilution for Western blot.

g) N-Methylprotoporphyrin Inhibition Experiments

Five milliliter cultures of E. Coli Δccm harboring either the pRGK333 orpRGK334 plasmid and pRGK332, or pRGK345 and pRGK349, were inoculatedwith 300 μl of overnight culture grown for 3 h to mid-exponential phase(A600=0.6). At this point, IPTG and NMPP (Frontier Scientific) wereadded to each culture; IPTG was added (1 mM) to induce the synthesis ofsystem I (pRGK333), system II (pRGK334), or ΔccmE (pRGK345) while NMPP(10 mM stock in 50% DMSO) was added to a final concentration of 0-100μM. After addition of IPTG and NMPP, cultures were grown an additionalhour before induction of cytochrome c₄:His (and ccmE from pRGK349) with0.2% arabinose. Cells were grown for an additional 3 h and thenharvested by centrifugation. Soluble protein was extracted with B-PERProtein Extraction Reagent (Pierce Biotechnologies; Rockfrod, Ill.) aspreviously described (Feissner et al., 2005).

h) Escherichia coli Membrane Fractionation

Escherichia Coli cultures were grown at 37° C. in LB media containingthe appropriate antibiotics. Soluble and membrane fractions wereprepared as previously described (Feissner et al., 2005). To isolateperiplasmic proteins from E. Coli, cells were harvested at 10 000 g for10 min at 4° C. and washed twice with 10 mM Tris pH 8 at roomtemperature. The resulting cell pellet was then resuspended in 1/10 ofthe starting culture volume in 100 mM Tris pH 8 containing 20% sucrose(w/v). The resuspension was stirred until warmed to 37° C. and lysozymewas added to a final concentration of 100 μg/ml. After 12 min ofstirring, 1 vol. of 100 mM EDTA was slowly added to 10 vols of cellsover a period of 2.5 min and stirred for additional 10 min. Spheroplastswere separated via centrifugation at room temperature for 10 min at 12000 g. The supernatant containing periplasmic proteins was saved. CrudeB-PER protein extractions were carried out as previously described(Feissner et al., 2005).

i) Heme Addition Experiments

Cultures of RK105 (E. coli ΔccmΔhemA) harboring pRGK333 (system I),pRGK332 (cytochrome c₄:6×His), and pHPEX2 (Varnado and Goodwin, 2004) orpRGK348 (system II) and pRGK332 were grown in LB overnight in thepresence of 300 μM aminolevulinic acid (ALA). 100 mL cultures werestarted from the overnight culture with a 1% inoculum in LB devoid ofALA for two and one-half hours. After two and one-half hours, the 100 mLcultures had exhausted their cellular supply of ALA and requiredexogenous heme (or ALA) for further growth. The ALA exhausted cultureswere divided into 5 mL aliquots to which IPTG (1 mM, to induce thesynthesis of the system I proteins) and heme (0 μM to 100 μM) (Sigma)were added. It was discovered that heme at greater than 60 μM wouldprecipitate over time with no IPTG (1 mM) present and at greater than100 μM in the presence of IPTG. After one hour, arabinose (0.2% toinduce the synthesis of cytochrome c₄:6×His) was added and cultures weregrown for an additional three hours. Cells were harvested and proteinwas extracted using B-PER as previously described (Feissner et al.,2006). Cytochrome c₄:6×His was purified from 200 μg of total proteinover nickel affinity resin to eliminate free heme. 20 μL of each samplewere subjected to SDS-PAGE, transferred to nitrocellulose, and hemestained as described above. Curve-fits and heme recovery calculationswere performed with the Origin scientific and analysis software package(OriginLab; Northhampton, Mass.) using the Hill equation as thecurve-fit model.

j) N-Methyl Protoporphyrin (NMPP) Inhibition Experiments

100 mL cultures of E. coli Δccm containing pRGK333 (system I), pRGK332(c₄:6×His), and pHPEX2 (Varnado and Goodwin, 2004) were inoculated with1% (v/v) from an overnight culture and grown with aeration at 37° C. toan OD₆₀₀ of approximately 0.5. The mid-log phase cultures were dividedinto 5 mL aliquots to which IPTG (1 mM, to induce the synthesis of thesystem I proteins and the chuA gene) and NMPP (0 μM to 100 μM) wereadded. After one hour 0.2% arabinose was added (to induce the synthesisof the B. pertussis c₄:6×His) and cultures were incubated an additionalthree hours. After harvesting cells by centrifugation, soluble proteinwas extracted with B-PER Protein Extraction Reagent (PierceBiotechnology) as previously described (Feissner et al., 2006).Cytochrome c₄:6×His was purified from 300 μg of total protein by nickelaffinity resin (Novagen) and 20 μL of each sample was subjected toSDS-PAGE, transferred to nitrocellulose and heme stained as describedbelow.

k) Metalloprotoporphyrin IX Addition Experiments

Overnight cultures of an E. Coli Δccm strain (or E. Coli ΔccmΔhemA)harboring either pRGK333 (system I) or pRGK348 (system II-chuA), pRGK332(cytochrome c₄:6×His), and pHPEX2 (Varnado and Goodwin, 2004) werediluted into fresh LB broth (containing the appropriate antibiotics and8 μM hemin for the E. Coli ΔccmΔhemA strain) and incubated with aerationat 37° C. until the OD₆₀₀ was approximately 0.5. The mid-log phasecultures were divided into 5 mL aliquots to which IPTG (1 mM) and ametalloprotoporphyrin IX (Zn (II), Sn (IV), Co (III), or Mn (III); 0 μMto 25 μM) were added. Arabinose (0.2%) was added after one hour andincubation continued for an additional three hours. Cells were harvestedand soluble protein was extracted using B-PER (Feissner et al., 2006).Cytochrome c₄:6×His was purified from 300 μg of total protein and 20 μLwas subjected to SDS-PAGE and transferred to nitrocellulose. Prior toheme stain and c4 immunoblot, the nitrocellulose blots were screened forfluorescence on an LAS-1000 plus Luminescent Image Analyzer CCD camerasystem (Fujifilm; Tokyo, Japan).

l) NMPP-ZnPPIX Combined Inhibition Experiments

Overnight cultures of an E. Coli Δccm strain harboring pRGK333 (systemI), pRGK332 (cytochrome c₄:6×His), and pHPEX2 were diluted into 100 mLof fresh LB broth containing the appropriate antibiotics and incubatedat 37° C. with aeration until an OD₆₀₀ of approximately 0.5 wasobtained. The cultures were divided into 5 mL aliquots and IPTG (1 mM)and ZnPPIX (5 μM and 12.5 μM) was added. Also at this time NMPP, at 60μM and 100 μM respectively, was added to each of these cultures andincubation continued for one hour. Arabinose (0.2%) was added andincubation continued for an additional three hours. Cells were harvestedby centrifugation and the soluble protein was extracted with B-PER, aspreviously described (Feissner et al., 2006). The soluble protein wasprocessed as for “metalloprotoporphyrin addition experiments”.

m) Other Methods

Heme stains were performed as described (Feissner et al., 2003) usingSuperSignal Femto chemiluminescent substrate (Pierce). Heme stainquantitation used LOLITA II (Low Light Test Array; raytestUSA;Wilmington, N.C.) for standardization of light intensity detection on anLAS1000 plus Luminescent Image Analyzer CCD camera system. For Westernblotting, extracts were first separated by 12% or 15% SDS-PAGE andelectroblotted onto Hybond-C nitrocellulose membranes (Amersham).Protein A peroxidase (Sigma-Aldrich) was used as the secondary label.Detection used the SuperSignal West Femto ECL detection system (Pierce).Chemiluminescence from heme stains and Western blots were detected usingan LAS-1000 plus Luminescent Image Analyzer CCD camera system(Fujifilm). Protein concentrations were determined using the BCA assay(Pierce) using BSA as a standard. The reduced (10 mM sodium dithionite)and oxidized (10 mM ammonia persulphate) absorption spectra wereobtained as previously described (Goldman et al., 1996) using Ni²⁺affinity-purified holocytochrome c₄:His. Protein concentrations weredetermined with the BCA assay kit (Pierce) using BSA as a standard.

TABLE 1 Nucleotide sequences of primers. Nu- Nucleotide Strain or cleo-Sequence Plasmid Primer tides 5′-3′ SEQ ID NO: E. coli Δccm- 60CGCCTGCGCG SEQ ID NO: 1 Δccm left ATACTACGTTC (RK103) AATCACCGCACGGCGAGTAGT GTAGGCTGGA GCTGCTTC E. coli Δccm- 60 ACGCTGAACG SEQ ID NO: 2Δccm right CAGGAGAGTG (RK103) GGTACAAATCA CCGGTAGCAC ATATGAATATCCTCCTTAG pRGK333 SysI- 32 TTGCAGATCTA SEQ ID NO: 3 (pSystemI) NtermTGCTTGAAGCC AGAGAGTTAC pRGK333 SysI- 33 CGGAATTCTTT SEQ ID NO: 4(pSystemI) Cterm TTATTTACTCT CCTGCGGCGA C pRGK345 CcmD- 30 GGCGAATTCTCSEQ ID NO: 5 (ΔccmE) Cterm ATATGGCCTCC TGCTGTTG pRGK345 CcmF- 33GACCCAGCCA SEQ ID NO: 6 (ΔccmE) Nterm TATGATGCCAG AAATTGGTAAC G pRGK346CcmG- 32 CCAATGAATTC SEQ ID NO: 7 (ΔccmH) Cterm CTTATTGTGCG GCCTCCTTACpRGK33O pBad24- 32 TATAAGCTTTT SEQ ID NO: 8 (pBad24- left TTGCCGATTTCcm^(r)) GGCCTATTGG pRGK33O pBad24- 27 ATCAGGCTGAA SEQ ID NO: 9 (pBad24-right AATCTTCTCTC cm^(r)) ATCCG pRGK331 c₄-pho- 27 AGTCGCTAGC SEQ ID NO:10 (pcytc₄: Nterm AGGAGGATTTC Pho) ATGAAG pRGK331 c₄-pho- 23 GTGCTGCAAGSEQ ID NO: 11 (pcytc₄: Cterm GCGATTAAGTT Pho) GG pRGK332 c₄- 48ACGGGTACCT SEQ ID NO: 12 (pcytc₄: 6xHis- CAGTGGTGGT 6xHis) CtermGGTGGTGGTG CCGCAAGCCC GCGGCGTA pRGK334 SysII- 32 GGAAAGATCTA SEQ ID NO:13 (pSystem Nterm TGAAGAATCTC II) AAAAGCCTGC pRGK334 SysII- 28TTCGAATTCCG SEQ ID NO: 14 (pSystem Cterm CGTCTAATAGG 11) GGTTGG pRGK347CcmE*- 33 GGTCCCATGG SEQ ID NO: 15 (pCcmE*) Nterm TATATGCGCTGCGCTCGAATAT C pRGK347 CcmE*- 35 CTGCTCGAGT SEQ ID NO: 16 (pCcmE*) CtermGATGCTGGGT CCTTATAAACA CTCG pRGK349 CcmE- 33 CAGGTACCGG SEQ ID NO: 17(pcytc₄: Nterm AGGCTGCATG Pho-CcmE) AATATTCGCCG TA pRGK349 CcmE- 48ACGCTGCAGT SEQ ID NO: 18 (pcytc₄: Cterm CAGTGGTGGT Pho-CcmE) GGTGGTGGTGTGATGCTGGG TCCTTATA E. coli ΔhemA- 60 CTATCAACGTT SEQ ID NO: 19ΔccmΔhemA left GGTATTATTTC (RK105) CCGCAGACAT GACCCTTTGTG TAGGCTGGAGCTGCTTC E. coli ΔhemA- 60 TGATGTACTGC SEQ ID NO: 20 ΔccmΔhemA rightTACTCCAGCCC (RK105) GAGGCTGTCG CGCAGAATCAT ATGAATATCCT CCTTAG

Example 1 Arabinose-Inducible B. Pertussis Cytochrome c Reporters in E.coli were Developed

Using the arabinose-inducible araB promoter from pBAD24 (Guzman et al.,1995), the ampicillin-resistance gene was replaced with achloramphenicol-resistance cassette from pHP45-Cm (Fellay et al., 1987)to make pRGK330 (FIG. 2A). Chloramphenicol rather than ampicillinresistance is necessary so these plasmids can be co-selected with thesystem I and II constructs (Amp^(r)) in the E. coli strain deleted forsystem I genes (Kan^(r); see below). A B. pertussis cytochromec:alkaline phosphatase (cycC-phoA) fusion was engineered downstream ofthe araB promoter and initially tested for alkaline phosphatase activityon plates with and without arabinose. This plasmid, pRGK331, whenpresent in the E. coli strain TB1, results in the production of anarabinose-inducible alkaline phosphatase activity. Heme staining, whichonly stains the covalently bound heme in c-type cytochromes separated bySDS-PAGE, indicated that a c-type cytochrome with the molecular mass ofapproximately 75 kDa was expressed after induction with 0.02% and 0.2%arabinose (FIG. 3, lanes 9 and 10). A lower molecular mass form(approximately 24 kDa) was observed that is similar in size to thenatural holocytochrome C₄.

A second cytochrome c₄ reporter was developed with a C-terminalhexahistidine tag. This reporter plasmid, pRGK332, in E. Coli results inthe arabinose-inducible production of a 24 kDa protein that possessesc-type heme (FIG. 3, lanes 4, 5). Thus, wild-type E. Coli can synthesizethe B. pertussis cytochrome c₄, presumably using its chromosomallyencoded system I pathway (see below).

Example 2 An E. coli Strain Deleted for all ccm (System I) Genes andComplementation by Plasmids Expressing Either System I or System IIGenes was Engineered and Validated

Using the procedure developed by Datsenko and Wanner (2000) on the E.Coli strain (RK103) with arabinose-inducible cytochrome c reporters, theeight genes comprising system I, ccmA through ccmH, were deleted andreplaced with a kanamycin-resistance cassette (see FIG. 2B for ccm genesat this locus) FIG. 4A shows that this ccm deletion strain, RK103, isunable to synthesize the holocytochrome c₄:alkaline phosphatase (lane 5)or holocytochrome c₄:His (lane 6), unlike the wild type (lanes 2, 3),indicating that the system I ccm genes are required for the synthesis ofthese cytochrome c₄ reporters. The ccmA through ccmH genes wereengineered into the pGEX vector (amp^(r)) such that CcmA is synthesizedas a fusion protein to glutathione S-transferase (GST) (FIG. 2B). Thisconstruct, pRGK333, when transformed into RK103 containing thereporters, was able to complement the cytochrome c synthesis defect.Both holocytochrome c₄:alkaline phosphatase and holocytochrome c₄:Hisare produced to levels approximately 10 times higher than wild type(FIG. 4A, lanes 8 and 10), partially due to the increased expression ofthe system I proteins (data not shown).

The minimal genes from system II that would carry out the biogenesis ofB. pertussis holocytochrome c reporters in RK103 were also engineered. Anatural ccsB-ccsA fused gene that is present in another proteobacterium,Helicobacter pylori (Tomb et al., 1997), was placed in frame to GST inpGEX-4T-1 and transformed into the E. coli with reporter strainsdescribed above. When present with pRGK331 in RK103, holocytochromec₄:alkaline phosphatase was produced (FIG. 4B, lane 8) at the samemolecular mass as when pRGK333, with system I, was present (FIG. 4B,lane 4). Likewise, when pRGK334 was present with pRGK332, a 24 kDaholocytochrome c₄ was produced (FIG. 4B, lane 10) at the same molecularmass as when pRGK333 was present (FIG. 4B, lane 6). To confirm that therecombinant cytochrome c₄ proteins had properties identical to thenatural molecules, the hexahistidine-tagged proteins were purified overNi²⁺. The absorption spectra of Ni²⁺-purified holocytochrome c₄:Hisshowed the characteristic spectra in the α/β and Soret region whetherassembled using system I (pRGK333, FIG. 5A) or system II (pRGK334, FIG.5B). Mass spectrometry analysis of Ni²⁺-purified holocytochrome c₄:His,when pRGK333 or pRGK334 is present, revealed a protein with a molecularmass of 23,659 Da (FIG. 5C), identical to the molecular mass of theholocytochrome c₄:His containing two heme molecules and a signalsequence cleaved after Ala27 (FIG. 5D). These results indicate that asingle polypeptide composed of the ccsB and ccsA ORFs can replace thefunction of all eight genes required for system I in E. coli.

Besides the covalent attachment of heme to the protein, as detected bythe heme stain and spectrometry, a characteristic of c-type cytochromesis that they typically fold into their native state after the heme isattached. This characteristic results in the susceptibility ofapocytochromes c to degradation by endogenous proteolysis when the hemeis not attached. To provide an additional line of evidence thatCcsBA-mediated assembly occurs in E. coli similar to the natural systemI in E. coli and system II in B. pertussis, antisera towards alkalinephosphatase and B. pertussis cytochrome c₄ were used to detect variousforms present in periplasmic shock fractions.

FIG. 6A, an immunoblot using alkaline phosphatase antibodies shows thatalkaline phosphatase was immunodetected only in extracts of strains thathad the cytochrome c₄:alkaline phosphatase reporter (lanes 2, 6, 10).Without a biogenesis system (FIG. 6A, lane 2), a single polypeptideapproximating the molecular mass of alkaline phosphatase (45 kDa) isdetected, suggesting that the majority of the apocytochrome c₄ portionis degraded when heme is not attached. When either system I (lane 6) orsystem II (lane 10) is present, two additional polypeptides are observedthat possess covalent heme (see heme stains in FIG. 4B, lanes 4 and 8).These polypeptides represent the full fusion protein and one that isdegraded down to the size of the mono-heme cytochrome c₄:alkalinephosphatase fusion protein (approximately 74 kDa and 62 kDarespectively, see below). In E. coli, either system I or heterologoussystem II attach heme and holocytochrome C₄ subsequently folds into astable protease-resistant form.

When antisera to cytochrome c₄ was used, each of the three alkalinephosphatase forms described above were detected (FIG. 6B, lanes 2, 6,10), although the lower molecular mass protein was less pronounced,suggesting that the product similar in size to the alkaline phosphatasepolypeptide still retains minor antigenic determinant(s) from thecytochrome c₄ C-terminus. (With the cytochrome c₄ antisera, acontaminating immunoreactive polypeptide slightly higher than 24 kDa isseen in all lanes, which can be used as an internal standard for proteinloaded.) When the cytochrome c₄:His-tagged protein is produced in astrain without a biogenesis system, no apocytochrome c₄ is detected(FIG. 6B, lane 1), whereas extracts from strains with either system I(lane 4) or system II (lane 8) produce significant amounts of detectablecytochrome c₄ polypeptide at 24 kDa. These extracts were furtherpurified over Ni2+ affinity columns and holocytochrome c₄ was detectableby heme stain (FIG. 6C) or immunoblot (FIG. 6D) only when either systemI or II is present. These results also confirm that the di-heme 24 kDacytochrome c₄ is partially proteolysed in E. coli to the mono-heme 12kDa forms. Mass spectrometry of Ni²⁺ affinity-purified holocytochromec₄, with pRGK333 present, revealed the 23,659 Da form (FIG. 5C) and twoproteins of mass 12,891 Da and 12,991 Da (not shown), consistent with asingle heme moiety and proteolysis after N125 and V126 (see FIG. 5D).The complete susceptibility of hexa-histidine-tagged apocytochrome c₄ toproteolysis but resistance of the holo forms in these recombinant cellssubstantiates that the ccsBA-encoded system II in E. coli is functional.

In E. coli, the CcsB and CcsA protein complex carries out the hemedelivery function and periplasmic cytochrome c₄-heme ligation functionswith no additional requirements, other than the reduction of thecysteinyl residues of the CXXCH motifs.

Example 3 Heme Limitation Highlighted Differences in Heme AcquisitionDynamics Between System I and System II

Using the reconstitution of system I and system II in a single geneticbackground (see Example 2) the ability of these two systems to deliverheme for holocytochrome c₄ synthesis was directly compared by measuringthe ability of each system to synthesize holocytochrome c₄:His underconditions of reduced cellular heme availability. To reduce availableheme levels, selected concentrations of the specific ferrochelataseinhibitor NMPP were used in the growth cultures (Moody and Dailey, 1985;Ferreira, 1994).

Cultures of RK103 harboring both pRGK333 (system I) and pRGK332(cytochrome c₄:His) were grown to early log phase, then IPTG (1 mM) wasadded to induce the synthesis of the system I proteins. At the sametime, NMPP was added to the growing cultures at final concentrations of0-100 μM in order to inhibit ferrochelatase, and subsequently reducecellular heme levels. One hour later, arabinose (0.2%) was added to thecultures to induce production of apocytochrome c₄:His. Cells were grownfor additional 3 h and harvested.

NMPP did not reduce the production levels of system proteins or ofapocytochrome c₄:alkaline phosphatase (data not shown). Cytochromec₄:His was extracted using B-PER bacterial protein extraction reagent(Pierce). As visualized via a heme stain, holocytochrome c₄:His signaldecreased gradually as NMPP concentration increased (FIG. 7A, lanes 1-9and 7B), but holocytochrome c₄:His production never went belowapproximately 38% of untreated wild-type levels (see FIG. 7A, lane 9).

When NMPP inhibition was carried out in RK103 harboring pRGK334 (systemII) and pRGK332 (cytochrome c₄:His) using the same protocol,holocytochrome c₄:His production dropped significantly at much lowerNMPP concentrations than was shown for system I (FIG. 8A lanes 1-9).Holocytochrome c₄:His production was completely abolished at less than20 μM NMPP in all trials. The dramatic difference between system I andsystem II suggests that system I is capable of acquiring heme atsignificantly lower heme levels than system II. It is proposed that thiscapability is due to the presence of an ABC transporter that is used insystem I (see FIG. 1). System II uses a single protein (CcsA) for hemedelivery, and our data suggest a significantly lower affinity for hemefor the CcsA protein.

Example 4 Holo-CcmE of System I can Function as a Heme Reservoir

A higher affinity for heme acquisition in system I is not sufficient toexplain the differences heme acquisition dynamics between systems I andII (see Example 3). One possibile explanation is that there is a ‘hemereservoir’ for system I, not present in system II. CcmE, a periplasmicheme chaperone, covalently binds heme in the periplasm and maypotentially function as a periplasmic heme storage protein. Antisera toCcmE was used to observe levels of CcmE in the membranes of IPTG-inducedand uninduced cells expressing pRGK333, or single gene deletions[pRGK345 (ΔccmE) and pRGK346 (ΔccmH)]. As shown in FIG. 9A, CcmE wasonly detected in extracts of strains with the ccmE gene (lanes 3, 4, 7,8). Additionally, CcmE is produced in the absence of IPTG in cellsexpressing pRGK333 and pRGK346, indicating a low level of constitutiveexpression (FIG. 9A, lane 3). This production is due to transcriptionfrom several minor promoters in ccmB through ccmC, upstream of ccmE andnot due to ‘leakiness’ of the Tac promoter that drives GST:CcmA-Hemestaining of membrane proteins from uninduced cells harboring pRGK333showed that significant holo-CcmE (FIG. 9B) was present in the membrane.The presence of CcmE bound heme in both a functional (pRGK333) system Ipathway and a system I pathway with a ccmH deletion (pRGK346) providedevidence of the ability of system I to store heme on CcmE.

To confirm the above results, pRGK332, the arabinose-induciblecytochrome c₄:His reporter, was modified to have a hexahistidine-taggedE. coli ccmE gene downstream of the gene for cytochrome c₄:His (FIG.2A). This plasmid, pRGK349, in E. coli RK103 also harboring pRGK345 (acomplete system I with a ccmE deletion), resulted in thearabinose-inducible production of the 24 kDa cytochrome c₄ (FIG. 10A) aswell as the arabinose-inducible production of CcmE (FIG. 10B). NMPPinhibition was carried out by the same method as in Example 3 with RK103expressing pRGK345 and pRGK349. A dramatic reduction in the amount ofholocytochrome c₄:His was detected at 100 μM NMPP (see FIGS. 10C and D)when compared with the results of Example 3 (pRGK333 and constitutivelyproduced CcmE, see FIG. 7B). These results suggest that holo-CcmErepresents up to 80% of the heme reservoir in system I cytochromes cbiogenesis. System II, with no storage mechanism, is unable to maintaina supply of heme for cytochromes c biogenesis.

Example 5 The Exogenous Porphyrin Approach: Characterization of an E.coli ΔccmΔhemA with a Porphyrin Porin

Using a strain of E coli with all eight ccmA-H genes deleted using akanamycin resistance cassette (see Example 2), a heme-dependent strainwas constructed. After screening for the excision of this kanamycinresistance cassette to obtain the Δccm kanamycin-sensitive strain(RK104), the hemA gene was replaced with a kanamycin resistancecassette, yielding the ΔccmΔhemA strain (RK105). Because the hemA genecodes for amino levulinic acid (ALA) synthase, the first committedenzyme in heme biosynthesis (see FIG. 11), the ΔccmΔhemA strain (RK105)required ALA in the growth media to form colonies. RK105 withrecombinant system I (pRGK333), or system II (pRGK334), also requiredexogenous ALA for growth (see FIG. 19). To determine if exogenous ALAfacilitates cytochromes c synthesis we transformed these strains withpRGK332, which expresses a C-terminally hexahistidine (6×) taggedBordetella pertussis cytochrome c₄ under the control of an arabinoseinducible promoter (see Example 1). E. coli ΔccmΔhemA with eitherpRGK333 (recombinant system I) or pRGK334 (recombinant system II) aswell as pRGK332 (arabinose inducible reporter) were unable to synthesizeholocytochrome c₄:6×His at the 60 μM ALA concentration (see FIG. 12lanes 1, 2, 6 and 7) but were able to synthesize holocytochrome c₄:6×Hisat higher ALA concentrations (see FIG. 12 lanes 3, 4, 5, 8, 9, and 10),indicating that exogenous ALA is required for growth and holocytochromec production in RK105.

To determine if exogenous heme rather than ALA could support growth, anovernight culture of E. coli ΔccmΔhemA, supplemented with 300 μM ALA,was used to inoculate [1% (v/v)] fresh LB medium containing differentconcentrations of heme (0 μM to 100 μM). Growth was not detected untilfour to five days after the original inoculation, even at high hemeconcentrations, and no holocytochrome c₄:6×His production was detectedin cultures that contained either the system I or system II plasmid andthe c₄:6×His reporter under these conditions.

Since the outer membranes of some strains of E. coli are poorlypermeable to heme, the heme porin from pHPEX2 (Varnado and Goodwin,2004) was expressed. The tetracycline-resistant pHPEX2 expresses thegene for the heme receptor (chuA) from E. coli O157:H7 using theIPTG-inducible lacUV5 promoter. ChuA is a member of a class ofrelatively nonspecific enterobacterial heme receptors that areTonB-dependent and facilitate heme acquisition from the environment andrecognize free heme and heme bound to a variety of proteins (see FIG.11). Growth of E. coli ΔccmΔhemA containing either pRGK333 or pRGK334and pHPEX2 was dependant on exogenous heme (see FIG. 13). Expression ofchuA (pHPEX2) allows growth to near wild-type levels, suggesting anefficient uptake of exogenous heme, whereas when the culture is depletedfor ALA and heme is not added, no growth is detectable (see FIG. 13 opensquares). The pHPEX2 also facilitates the heme-dependent production ofthe B. pertussis c₄:6×His when the plasmids with system I or system IIare present (see below).

To directly examine the difference in heme acquisition between systems Iand II, varying concentrations of exogenous heme were supplied to E.coli ΔccmΔhemA, expressing ChuA with pRGK332 and either system plasmid.Overnight starter cultures supplemented with 300 μM ALA were used toinoculate [1% (v/v)] LB devoid of ALA and incubated for two and one-halfhours to exhaust cellular ALA (and heme). The ALA-exhausted cultureswere then grown in the presence of IPTG (1 mM), arabinose (0.2%), andheme (0 μM to 100 μM). The cytochrome c4 acts as a trap, allowingquantitation of the levels of heme that have fluxed through each system.Cytochrome c₄:6×His was purified over nickel chelating resin toeliminate free heme and quantitated by heme stain (FIG. 14A for system 1and 14C for system II). For system I, it was determined that maximumsynthesis of holocytochrome c₄:6×His occurs at less than 10 μM heme,therefore, all subsequent experiments using system I were carried out atheme levels between 0 μM and 10 μM. Averaged over 4 trials for system I,holocytochrome c₄:6×His levels were restored to 50% (of maximum levelsachieved with exogenous heme) at 1.9 μM+/−0.4 μM heme (FIG. 14B). Forexperiments with system II (CcsBA), an increase in holocytochromec₄:6×His signal was also observed as heme concentration increased, withheme levels of 80 μM to 100 μM reaching maximum synthesis (FIG. 14C).Averaged over 3 trials, holocytochrome c₄:6×His levels reached 50% ofmaximum synthesis at 54.4 μM+/−18.2 μM heme for system II (FIG. 14D).The apparent affinity for heme is at least twenty fold higher for systemI than system II.

Example 6 Zinc Protoporphyrin IX (ZnPPIX) is not Incorporated into theB. Pertussis Cytochrome c₄:6×His Biogenesis Reporter

The chemical properties of iron may not be uniquely critical for itsattachment to apocytochrome c during cytochromes c biogenesis. To testwhether any of the cytochromes c biogenesis systems can incorporateother metal porphyrins, four metalloporphyrins were chosen to screen forincorporation into the into the CXXCH motif of a c-type cytochrome:ZnPPIX, SnPPIX, MnPPIX, and CoPPIX. These four metalloporphyrins weretested to determine whether heme can be replaced by othermetalloporphyrins in the c-type cytochrome (c₄:6×His) reporter. Culturesof E. coliΔccmΔhemA containing pRGK333 (system I), pRGK332 (c₄:6×His),and pHPEX2 were grown overnight in 300 μM ALA and subcultured into freshLB medium containing 8 μM heme and grown to an OD₆₀₀ of 0.5. IPTG andmetalloporphyrin (8 μM, 12.5 μM, or 25 μM) were then added and growthcontinued for one hour. Arabinose was added to 0.2% to induce thesynthesis of the c₄:6×His and growth continued for three more hoursbefore cells were harvested. The cytochrome c₄:6×His proteins wereaffinity purified over nickel columns, subjected to SDS-PAGE andtransferred to nitrocellulose and subsequently heme stained. Asexpected, heme was detected on c₄:6×His when either 8 μM or 25 μM hemealone was added (FIG. 15 lanes 1 and 2, respectively). When ZnPPIX waspresent with 8 μM heme, decreasing amounts of holocytochrome c₄ weredetected as the ZnPPIX concentration increased (FIG. 15 lanes 3-5). At25 μM ZnPPIX (see FIG. 15 lane 5) the level of heme on c₄:6×His wasnearly undetectable. Concentrations of ZnPPIX above 25 μM did notfurther reduce the level of detectable heme (not shown). SnPPIX alsoreduced the level of detectable heme on c₄:6×His (see below). However,neither CoPPIX nor MnPPIX had any affect on the levels of cytochromes c(not shown).

ZnPPIX (and SnPPIX), when present with 8 μM heme, may compete with hemefor ChuA-dependent transport into the cell. Using an E. coli Δccm strain(RK103) that has endogenous heme production, it was tested whetherZnPPIX (and SnPPIX) caused a reduction in holocytochrome c4 levelsdetectable by heme stain. When E. coliΔccm with pRGK333 (system I),pRGK332, and pHPEX2 were treated with ZnPPIX, a decrease inholocytochrome c₄:6×His was detected as the concentration of ZnPPIX wasincreased (FIG. 16A left panel, lanes 1-5). E. coli Δccm with system IIexpressing chuA also showed a decrease in holocytochrome c₄:6×His withZnPPIX (FIG. 16B left panel, lanes 1-6).

The three other metal protoporphyrins, SnPPIX, MnPPIX, and CoPPIX, werealso tested in the E. coli Δccm background with system I or II. E. coliΔccm with pRGK332 (cytochrome c₄:6×His), expressing chuA and eithersystem I or II, showed a decrease in holocytochrome c₄:6×His as theconcentration of SnPPIX was increased (FIG. 20A lanes 1-5 and 20B lanes1-5). Addition of MnPPIX or CoPPIX (up to 100 μM) showed no decrease inthe level of heme on c₄:6×His, suggesting that these are notincorporated and are not inhibitors (see below). The reduction ofholocytochrome c₄:6×His with system I required significantly higherconcentrations of SnPPIX than system II, in these experiments. Theconcentration of SnPPIX compared to ZnPPIX required for holocytochromec₄:6×His reduction was also higher for both systems. The concentrationof ZnPPIX required for 50% inhibition of system I was approximately 2 μMand for system II was approximately 25 nM, whereas the concentration ofSnPPIX required for 50% inhibition of system I was approximately 65 μMand for system II was approximately 18 μM.

It was determined that ZnPPIX does not react with the chemiluminescentsubstrate used to stain for heme on holocytochrome c4 (unpublished). Theabsence of a heme stain could indicate that ZnPPIX is either 1)competing with heme and is being incorporated into c₄:6×His, or 2) isspecifically inhibiting c-type cytochrome biogenesis (i.e. attachment ofheme).

Cytochrome c₄ covalently bound to ZnPPIX would be highly fluorescent, aproperty of ZnPPIX proteins. We were unable to detect fluorescence ofZnPPIX in purified c₄:6×His preparations from these experiments,suggesting that ZnPPIX is not incorporated. To confirm this, cytochromec₄ immunoblots were performed on nickel affinity purified c₄:6×His. IfZnPPIX is incorporated into the apocytochrome c it was expected that theholocytochrome would be stable and not subject to natural proteolysis.Cultures of E. coli Δccm harboring pRGK332 (c₄:6×His) and either systemI or II that express chuA were grown and treated as described above.When antisera to the B. pertussis cytochrome c₄ was used (FIGS. 16A andB right panels) a decrease in the levels of c₄:6×His was detected forboth system I (FIG. 16A right panel lanes 6-10) and system II (FIG. 16Bright panel lanes 7-12). These results suggest that ZnPPIX is notincorporated into the cytochrome c₄:6×His by either system but rather isinhibiting biogenesis. Similar results were observed when SnPPIX wasused (FIG. 20A lanes 6-10 and 20B lanes 6-10), which also suggest thatSnPPIX is not being incorporated into cytochrome c₄:6×His by system I orII.

To confirm that ZnPPIX is not incorporated into the cytochrome c₄,visible absorption spectra were obtained of nickel purified cytochromec₄:6×His isolated from Δccm harboring pRGK333 (system I), pRGK332(c₄:6×His), and pHPEX2 grown with 8 μM ZnPPIX (see FIG. 17A). Note thatat this concentration, approximately 20% of wild type levels ofholocytochrome c₄:6×His is produced (see FIG. 16A, lane 3). The sodiumhydrosulfite reduced α peak at 552 is characteristic of cytochrome C₄with a c-type linkage to heme. If ZnPPIX were incorporated we would haveexpected β/α peaks at 549 and 585, respectively. In addition, ESI-MSanalysis of this same protein preparation showed that the holocytochromec₄*(12 kDa proteolytic fragment) contained only heme, as ZnPPIXincorporation would have yielded a protein that was 10 mass units larger(FIG. 17B and inset). These results confirm that ZnPPIX is notincorporated into cytochrome c₄:6×His but rather inhibits biogenesis.

To rule out that ZnPPIX is not affecting some basic cellular processes,growth studies were performed with E. coli Δccm harboring pRGK333(system I), pRGK332 (c₄:6×His), and pHPEX2. Cultures with either 12.5 μMor 25 μM ZnPIX showed no decrease in the rate or yield of growth whencompared to the same strain without ZnPPIX (FIG. 21). In addition, usinga plasmid with c₄:Pho [B. pertussis cytochrome c₄ alkaline phosphatasefusion that is induced with arabinose (see Example 1), alkalinephosphatase was detectable at equivalent levels in the presence orabsence of ZnPPIX (FIG. 22A lanes 6 and 7). These results indicate thatZnPPIX is not inhibiting transcription, translation, or secretion ofcytochrome C₄, further suggesting that ZnPPIX is specifically inhibitingsome step(s) in c-type cytochrome biogenesis.

Example 7 ZnPPIX Specifically Inhibits System I c-Type CytochromeBiogenesis after HoloCcmE Synthesis

Previously, it was determined that ZnPPIX is specifically inhibitingsome step(s) in c-type cytochrome biogenesis (see Example 6). To examinewhere ZnPPIX is inhibiting system I c-type cytochrome biogenesis, thepresence of heme on cytochrome c₄:6×His was assayed when both N-methylprotoporphyrin (NMPP) and ZnPPIX were included in the culture of E. coliΔccm containing pRGK333 (system I), pRGK332 (c₄:6×His), and pHPEX2. WhenNMPP, a potent inhibitor of ferrocheletase that can completely abolishheme synthesis, was added to the culture of E. coliΔccm containingpRGK333 (system I) and pRGK332 (c₄:6×His), holocytochrome c synthesiswas reduced to a basal level of approximately 38% (see Example 3). Thisresult was shown to be due to the ability of the CcmE protein to act asa reservoir for heme, thus permitting residual (38%) synthesis ofholocytochrome c₄:6×His when 100 μM NMPP was added to the culture (seeExample 4). Thus, in these experiments holoCcmE is present at levelsthat allow 38% of holocytochrome c₄ production when ferrocheletase isinhibited. If ZnPPIX inhibits synthesis significantly more than NMPP, itmust be acting after the formation of this heme reservoir since someholoCcmE is present at the time of ZnPPIX addition (see FIG. 11).

Cultures of E. coliΔccm containing pRGK333 (system I), pRGK332(c₄:6×His), and pHPEX2 were grown to mid-log phase and NMPP (60 μM and100 μM) and IPTG (1 mM) were added. Following incubation for 30 minutes,ZnPPIX (5 μM and 12.5 μM) was added, independently, to these culturesand incubation continued for 30 additional minutes. Arabinose (0.2%) wasadded to induce the expression of cytochrome c₄:6×His and growthcontinued for three more hours. In addition, inhibition experiments wereperformed that contained either 0 μM to 100 μM NMPP or 0 μM to 25 μMZnPPIX alone. Cells were harvested and protein was extracted usingB-PER. Cytochrome c₄:6×His was nickel affinity purified and quantitatedby heme stain (FIG. 18). When both NMPP and ZnPPIX were present theholocytochrome c₄:6×His levels dropped from approximately 54% with NMPPalone (FIG. 18, 60 μM NMPP) to approximately 7% at 60 μM NMPP/5 μMZnPPIX and from approximately 30% (FIG. 18, 100 μM NMPP) to 0% at 100 μMNMPP/5 μM ZnPPIX. This result is consistent with previous data showingthat ZnPPIX inhibits holocytochrome c₄:6×His production to nearlyundetectable levels (see Example 6).

ZnPPIX is inhibiting downstream of holoCcmE since this “heme reservoir”is no longer available for cytochrome c₄ biogenesis. The WWD containingprotein CcmF may the target for ZnPPIX (see FIG. 11). If the target forZnPPIX is a heme binding protein (site), then exogenous heme shouldcompete with this inhibition (i.e. ZnPPIX binding). To test this, wecultured E. Coli Δccm with system I, ChuA, and cytochrome c₄:Pho grownwith 12.5 μM ZnPPIX and increasing concentrations of additional heme andobserved a corresponding increase in holocytochrome c₄:Pho (FIG. 22Blanes 1-5). The same heme stained polypeptides were confirmed to be fulllength cytochrome c₄:Pho fusion proteins by Western blot (FIG. 22A, lane1-5). ZnPPIX is a specific inhibitor of c-type cytochrome biogenesis byeither system I or system II, but heme is able to compete with ZnPPIXinhibition.

Example 8 Previously Developed Recombinant Cytochrome c (His6 Tagged)Reporters May be used to Develop High Throughput Screening Technologyfor Cytochrome c

Many strains, plasmids, and growth conditions have already beeninvestigated to detect cytochrome c reporters at the subpicomole level.These assays are from less than one milliliter cultures. These reagentsmay be used to optimize ECL-(chemiluminescent-) based detection of thecytochrome c product in 96 & 384 well microtiter plate format, as aprimary screen. The primary screen may involve induction with arabinoseof the cytochrome c:His reporter (see Example 1) after inhibitors areadded; this screen may capture inhibitors of cytochrome c and hemesynthesis, secretion, translation, and transcription.

Preliminary data on a subset of conditions using 96-well plates and aluminometer indicates that the ECL-(chemiluminescent-) based detectionof cytochrome c in whole E. coli cells may serve as HTS format.Recently, 96 well assays were piloted using a Luminoscan plateluminometer and Pierce ECL reagents. It was determined with theLuminoscan that whole cells expressing the cytochrome c reporter couldbe used. Pure cytochrome c₄ and whole E. coli cells synthesizingcytochrome c4 were detected in 96 well opaque (white) plates (FIG. 10).The detection sensitivity of pure cytochrome c₄ surpassed the Fuji CCDdetection limits (see FIG. 23), well #11D, where 0.2 ng is detected at2076 RLU=relative light units). As shown in FIG. 23, E. coli that didnot contain a pathway (columns 4-6) or did not have the cytochrome c₄plasmid (columns 1-3) exhibited significantly less luminescence thancells synthesizing holocytochrome c (columns 7-9). Although it wasdetermined that some factor in the LB culture was quenching the signalwhen more than 15 μl of LB culture was used, assays with 10 μl cultureor less (in LB media) showed significant signal.

To provide confidence that the ECL signal from this microtiter plateassay is emanating from the cytochrome c₄, rather than some unknownsource, one ml of culture in LB, using the same strains as used in the96 well plate assays, were sonicated, unbroken cells centrifuged, andsupernatant (15 μl) in LB was run on a native PAG and ECL-stained (FIG.24). FIG. 24 shows that the major ECL signal was from the cytochrome c₄and that extracts of E. coli cells not synthesizing cytochrome c₄ showedno signals.

A secondary screening method for detection of holocytochrome c4 may usehigh-titer antisera to cytochrome c4. It is common that c-typecytochromes are degraded naturally if the heme is not attached.Cytochrome c4 antisera have been used to show that no cytochrome c4 isimmunodetected when a functional system is not present, or is inhibitedby a non-iron metal porphyrin (see Examples 2 and 6). Purified anti-serato cytochrome c4 may offer another capability for detection ofholocytochrome c (and thus small molecule inhibitors of the pathways).Western detection in combination with heme stains may be used as asecondary screening for cytochromes c, with the capacity to complete1000 assays in a 2-3 week period

A cytochrome c: alkaline phosphatase (PhoA) fusion reporter may also beused as an additional secondary screening to confirm specific inhibitionof cytochrome c synthesis. Cytochrome c: PhoA fusion is synthesized as aholocytochrome c and active alkaline phosphatase fusion protein (seeExample 1). When inhibited (or no system is present) the fusion proteindoes not possess heme. Moreover, the cytochrome c₄ domain is degradedbut the alkaline phosphatase component has wild-type activity and it isdetected by western blot at the same size as alkaline phosphatase. Theseproperties will be used to confirm inhibition by small molecules and todemonstrate specificity towards the cytochrome c assembly system(s). ThePhoA fusion analysis may confirm inhibition of cytochrome c (or heme)synthesis by detecting the natural degradation of the cytochrome ccomponent (because heme is not attached), and the alkaline phosphatase(PhoA) component is used to show that transcription, translation, orsecretion is not the target for the putative small molecule inhibitor.These assays have shown that the Zn and Sn PPIXs are specific largemolecule inhibitors of systems I and II pathways (see example 7).

REFERENCES

All references cited in the preceding text of the patent application orin the following reference list, to the extent that they provideexemplary, procedural, or other details supplementary to those set forthherein, are specifically incorporated by reference to the same extent asif each individual publication or patent application was specificallyand individually indicated to be incorporated by reference.

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1. A method for identifying a compound that inhibits cytochrome csynthesis in a bacterial cell, the method comprising: a. contacting atransfected bacterial cell with a compound, the bacterial cell beingtransfected with a first expression vector encoding Ccm proteins and asecond expression vector encoding a cytochrome c reporter protein,wherein the bacterial cell has a chromosomal disruption in the regionencoding the Ccm proteins; and b. determining the amount of cytochrome creporter protein produced in the presence of the compound relative tothe amount produced in the absence of the compound, wherein a decreasein amount is an indication that the compound inhibits the synthesis ofcytochrome c.
 2. The method of claim 1, wherein the transfectedbacterial is a gamma proteobacterium cell.
 3. The method of claim 2,wherein the transfected bacterial cell is an Escherichia coli cell. 4.The method of claim 1, wherein the Ccm proteins coded by the firstexpression vector are from a gamma proteobacterium.
 5. The method ofclaim 4, wherein the Ccm protiens are the CcmA-H proteins of Escherichiacoli.
 6. The method of claim 1, wherein the second expression vectorencodes a cytochrome c:alkaline phosphate fusion protien or a cytochromec:6xHis fusion protien.
 7. The method of claim 6, wherein the cytochromec protien is cytochrome c₄ from Brodetella pertussis.
 8. The method ofclaim 1, wherein the coding region of the first expression vector isoperably linked to a first inducible promoter and the coding region ofthe second expression vector is operably linked to a second induciblepromoter.
 9. The method of claim 8, wherein the first promoter isinduced by IPTG and the second promoter is induced by arabinose.
 10. Themethod of claim 1, wherein the transfected bacterial cell grows in thepresence of exogenous amino levulinic acid (ALA).
 11. The method ofclaim 1, wherein the transfected bacterial cell further comprises achromosomal disruption in the region encoding the HemA protein.